Self-assembled micelles prepared from bio-based hydroxypropyl methyl cellulose and polylactide amphiphilic block copolymers for anti-tumor drug release

被引:32
|
作者
Lu, Aijing [1 ]
Petit, Eddy [1 ]
Jelonek, Katarzyna [2 ]
Orchel, Arkadiusz [3 ]
Kasperczyk, Janusz [2 ,3 ]
Wang, Yuandou [4 ]
Su, Feng [4 ]
Li, Suming [1 ]
机构
[1] Univ Montpellier, Inst Europeen Membranes, ENSCM, CNRS,IEM,UMR 5635, Montpellier, France
[2] Polish Acad Sci, Ctr Polymer & Carbon Mat, Curie Sklodowska 34 St, PL-41819 Zabrze, Poland
[3] Med Univ Silesia, Sch Pharm, Dept Biopharm, Div Lab Med Sosnowiec, 8 Jednosci Str, PL-41200 Sosnowiec, Poland
[4] Qingdao Univ Sci & Technol, Inst High Performance Polymers, Qingdao 266042, Peoples R China
关键词
Hydroxypropyl methyl cellulose; Polylactide; Self-assembly; Paclitaxel; Micelle; Drug release; Cytotocompatibility; CYTOTOXICITY; FILOMICELLES; BEHAVIORS; DELIVERY; ASSAY;
D O I
10.1016/j.ijbiomac.2020.03.094
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Fully bio-based amphiphilic diblock copolymers were synthesized from hydroxypropyl methyl cellulose (HPMC) and amino-terminated poly(L-lactide) (PLLA) or poly(L-lactide-co-DL-lactide) (PLA) by reductive amination. The resulting HPMC-PLLA and HPMC-PLA copolymers with various hydrophobic block lengths were characterized by NMR, DOSY-NMR and FT-IR. Micelles were obtained by self-assembly of copolymers in aqueous medium. The micelles are spherical in shape, and the micelle size ranges from 150 to 180 nm with narrow distribution. The critical micelle concentration decreases with increasing PLA block length. Paclitaxel was loaded in micelles. Enhanced drug loading is obtained with increase of PLA block length. A biphasic release profile is observed with a burst of 40% followed by slower release up to 80%. MTT assay indicates the good cytocompatibility of HPMC-PLA micelles. SRB assay shows a significant cytotoxicity of paclitaxel-loadedmicelles against SK-BR-3cells. It is thus concluded that bio-based HPMC-PLA block copolymers could be promising nano-carrier of anti-tumor drugs. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:39 / 47
页数:9
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